Lead Production Supervisor

Catalent; Windsor; On-site; CAD 84,000 - 107,000; Full time

Benefits offered by this job

Comprehensive Benefits Package (Health

Registered Pension Plan (RPP)

Employee Reward & Recognition

Tuition reimbursement

Job summary

Catalent in Windsor, Ontario, is seeking a Lead Production Supervisor for 100% on-site work at the Windsor manufacturing site. You will lead and coach shift supervisors, hourly staff and supporting departments to achieve safe, compliant and efficient operations.

Key duties include tracking SQDC metrics, maintaining an action log for audits, developing training programs, guiding continuous improvement, and coordinating daily shift handovers and meetings.

Qualifications

• 1+ year of supervisory experience in manufacturing.
• Strong leadership, communication and interpersonal skills.
• Experience in pharmaceutical manufacturing or GMP is an asset.
• Knowledge of automation systems is an asset.

Responsibilities

• Track SQDC metrics; address deviations in safety, quality, delivery and cost.
• Monitor and maintain an action log to enhance compliance and audit readiness.
• Develop and coordinate departmental classroom training programs and monitor qualifications.
• Lead special projects as defined by the Production Manager.
• Coach and mentor production supervisors, including advising and timely feedback.
• Provide supervisor coverage for vacations and training.
• Support shift handover meetings and department communication with daily shift meeting agenda.
• Perform other duties as assigned.

Skills

Leadership

Supervisory experience

Communication

Interpersonal skills

Team mentoring

Microsoft Office

Education

High School Diploma

Bachelor’s degree in Life Sciences

Tools

Microsoft Office Suite

Job description

Position Summary

This position is located in Windsor, Ontario, at the Windsor manufacturing site. The role is 100% on‑site and involves softgel development and manufacturing for the Pharmaceutical and Consumer Health industries.

Reporting to the Department Production Manager, the Lead Production Supervisor will be responsible for efficient manufacturing operations, health and safety, operational excellence, quality and regulatory compliance, customer requirements, and organizational goals. The position includes leading and coaching shift supervisors, hourly employees and staff across supporting departments.

Work Schedule: Shifts: Regular working hours: 8:00 AM – 4:30 PM or 8:30 AM – 5:00 PM with a 30‑minute unpaid lunch.

The Role

• Track SQDC metrics; address deviations in safety, quality, delivery, and cost.
• Monitor and maintain an action log to enhance compliance and audit readiness.
• Develop and coordinate departmental classroom training programs and monitor qualifications.
• Lead special projects as defined by the Production Manager.
• Coach and mentor production supervisors, including advising, guiding, and providing timely feedback.
• Provide supervisor coverage for vacation, extended absence, and training.
• Support shift handover meetings and department communication by creating, updating, and maintaining a daily shift meeting agenda.
• Perform other duties as assigned.

Candidate Qualifications

• High School Diploma, GED/CAEC, or equivalent. Bachelor’s degree in Life Sciences (Chemistry, Biology) or related field is preferred.
• At least 1 year of supervisory experience in a manufacturing environment, ensuring safety, quality, and productivity. Strong leadership, communication, and interpersonal skills, with experience in a diverse workforce and continuous improvement culture.
• Experience in manufacturing, pharmaceutical and/or GMP facilities is an asset.
• Knowledge of pharmaceutical manufacturing processes, flexible and able to work in a fast‑paced team environment.
• Strong technical background and computer skills, including Microsoft Office Suite (Outlook, Excel, Access, Word).
• Strong interpersonal skills to influence and motivate others at all levels.
• Knowledge of automation systems is an asset.
• Leadership experience at Catalent, such as participation in Catalent‑sponsored programs (NGGL, GOLD, LEAD Now, GM Excellence, GROW), may be considered in lieu of external experience.
• For non‑Canadian credentials, a Canadian equivalency evaluation (e.g., WES) is required.
• Manual dexterity for tasks such as handling, keyboard use, and physical tasks may be required; the position involves standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, mandatorily requiring good vision and possible chemical exposure.

Pay

The final salary offered to a successful candidate may vary within the range $84,000 - $107,000, dependent on factors such as experience, industry background, skill set, education, and business needs.

Benefits

• Comprehensive Benefits Package (Health, Dental, Vision, & Life Insurance)
• Registered Pension Plan (RPP) with employer contributions.
• Employee Reward & Recognition programs.
• Opportunities for professional and personal development, including tuition reimbursement.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

Accommodation: If you require reasonable accommodation for any part of the application or hiring process due to a disability, please send your request to [e-mail] including the job number, title, and location.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.